SEQUOIA DIAGNOSTIC ULTRASOUND SYSTEM

SEQUOIA DIAGNOSTIC ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K041319) manufactured by Siemens Medical Solutions USA, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 6, 2004. Regulation: 8.